|
ENST00000356839.10:c.819A>C
MANE Select
|
ENSP00000349297.5:p.Gly273=
|
|
|
ENST00000322910.9:c.*774A>C
|
ENSP00000325395.5:n.*774A>C
|
|
|
ENST00000350303.9:c.753A>C
|
ENSP00000344152.5:p.Gly251=
|
|
|
ENST00000356839.9:c.819A>C
|
ENSP00000349297.5:p.Gly273=
|
|
|
ENST00000543245.6:c.888A>C
|
ENSP00000438689.2:p.Gly296=
|
|
|
ENST00000577191.5:n.991A>C
|
|
|
|
ENST00000581378.5:c.537A>C
|
|
|
|
ENST00000582379.1:n.203A>C
|
|
|
|
NM_000018.3:c.819A>C
|
NP_000009.1:p.Gly273=
|
|
|
NM_001033859.2:c.753A>C
|
NP_001029031.1:p.Gly251=
|
|
|
NM_001270447.1:c.888A>C
|
NP_001257376.1:p.Gly296=
|
|
|
NM_001270448.1:c.591A>C
|
NP_001257377.1:p.Gly197=
|
|
|
XM_006721516.2:c.819A>C
|
XP_006721579.2:p.Gly273=
|
|
|
XM_011523829.1:c.819A>C
|
XP_011522131.1:p.Gly273=
|
|
|
XM_011523830.1:c.819A>C
|
XP_011522132.1:p.Gly273=
|
|
|
XR_934021.1:n.926A>C
|
|
|
|
XR_934022.1:n.926A>C
|
|
|
|
XR_934023.1:n.926A>C
|
|
|
|
XM_006721516.3:c.819A>C
|
XP_006721579.2:p.Gly273=
|
|
|
XM_011523829.2:c.819A>C
|
XP_011522131.1:p.Gly273=
|
|
|
XM_011523830.2:c.819A>C
|
XP_011522132.1:p.Gly273=
|
|
|
XM_024450741.1:c.819A>C
|
XP_024306509.1:p.Gly273=
|
|
|
XR_934021.2:n.878A>C
|
|
|
|
XR_934022.2:n.878A>C
|
|
|
|
XR_934023.2:n.878A>C
|
|
|
|
NM_000018.4:c.819A>C
MANE Select
|
NP_000009.1:p.Gly273=
|
|
|
NM_001033859.3:c.753A>C
|
NP_001029031.1:p.Gly251=
|
|
|
NM_001270447.2:c.888A>C
|
NP_001257376.1:p.Gly296=
|
|
|
NM_001270448.2:c.591A>C
|
NP_001257377.1:p.Gly197=
|
|
